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Average Ratings 0 Ratings

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ease
features
design
support

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Description

CIMS Global delivers advanced data science platforms and eClinical solutions that are set to transform the landscape of clinical trials by enhancing the quality, efficiency, and speed of processes like data acquisition, processing, analysis, monitoring, and regulatory submissions. Their offerings feature groundbreaking tools such as CRE, DDM, DMC-HUB, and eBinder, as well as a comprehensive eClinical Suite that facilitates data collection, analytics, and clinical functions throughout all phases of a trial. CRE serves as a multi-tenant, validated Statistical Computing Environment specifically designed for compliant analysis of clinical data, leveraging R, RShiny, and the RStudio IDE within a secure framework ready for audits that aligns with 21 CFR Part 11 and GxP regulations. DDM stands out as a patented Dynamic Data Monitoring platform that visualizes cumulative treatment effects on a trial radar screen while also forecasting the likelihood of a trial’s success or failure. Additionally, the integration of these innovative solutions positions CIMS Global at the forefront of clinical trial technology, ensuring that researchers can achieve optimal outcomes in their studies.

Description

Judi is an innovative cloud-based platform designed for clinical trial collaboration, aimed at enhancing, securing, and streamlining intricate workflows among sponsors, CROs, trial sites, and various partners. This platform encompasses a comprehensive array of trial functions, including endpoint and event adjudication, central eligibility assessments, data safety monitoring, remote oversight, medical imaging, site/user qualification, and personalized workflows through Judi Flex. By replacing outdated manual processes, spreadsheets, unmonitored emails, and isolated file-sharing methods, Judi creates a cohesive and compliant workspace where every document, communication, image, query, and decision flows through secure and traceable channels. Among its robust features are role-based access controls, audit trails, real-time messaging, efficient query management, customizable dashboards, worklists, flexible document submission and review processes, eCRFs with edit checks, and advanced reporting tools, which collectively enhance the efficiency and accuracy of trial data collection, review, and reporting. Furthermore, this platform’s comprehensive approach ensures that all stakeholders can collaborate seamlessly, leading to improved outcomes and faster trial timelines.

API Access

Has API

API Access

Has API

Screenshots View All

Screenshots View All

Integrations

R
RStudio

Integrations

R
RStudio

Pricing Details

No price information available.
Free Trial
Free Version

Pricing Details

No price information available.
Free Trial
Free Version

Deployment

Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook

Deployment

Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook

Customer Support

Business Hours
Live Rep (24/7)
Online Support

Customer Support

Business Hours
Live Rep (24/7)
Online Support

Types of Training

Training Docs
Webinars
Live Training (Online)
In Person

Types of Training

Training Docs
Webinars
Live Training (Online)
In Person

Vendor Details

Company Name

CIMS Global

Founded

2004

Country

United States

Website

cims-global.com

Vendor Details

Company Name

Judi

Founded

2004

Country

United States

Website

www.judi.io

Product Features

Clinical Trial Management

21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning

Data Science

Access Control
Advanced Modeling
Audit Logs
Data Discovery
Data Ingestion
Data Preparation
Data Visualization
Model Deployment
Reports

Electronic Data Capture

Audit Trail
CRF Tracking
Data Entry
Data Verification
Distributed Capture
Document Imaging
Document Indexing
Forms Management
Remote Capture
Study Management

Product Features

Clinical Trial Management

21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning

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